6638-91-1 Usage
Description
2-(PIPERIDINOMETHYL)-1-NAPHTHOL is a chemical compound characterized by the molecular formula C17H19NO. It features a naphthol group, an aromatic alcohol, linked to a piperidinomethyl group, which includes a piperidine ring. 2-(PIPERIDINOMETHYL)-1-NAPHTHOL is recognized for its potential in research and pharmaceutical applications, primarily serving as a building block in the synthesis of a variety of organic molecules. Its distinctive structure and properties also render it a valuable asset for exploring the behavior of organic compounds across different settings, with possible implications in drug development and as a catalyst in chemical reactions.
Uses
Used in Pharmaceutical Research and Development:
2-(PIPERIDINOMETHYL)-1-NAPHTHOL is utilized as a key intermediate in the synthesis of pharmaceutical compounds, contributing to the creation of new drugs. Its unique structure allows for specific interactions with biological targets, potentially leading to the development of innovative therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, 2-(PIPERIDINOMETHYL)-1-NAPHTHOL is employed as a building block for the assembly of complex organic molecules. Its presence in these molecules can influence their reactivity, stability, and overall properties, making it a versatile component in the synthesis of a wide range of organic compounds.
Used in Catalyst Design:
2-(PIPERIDINOMETHYL)-1-NAPHTHOL's structure and properties also suggest its potential use in the design of catalysts for chemical reactions. Its ability to participate in various chemical processes could enhance the efficiency and selectivity of reactions, which is particularly important in industrial applications where catalyst performance is crucial.
Used in Chemical Research:
2-(PIPERIDINOMETHYL)-1-NAPHTHOL serves as a valuable tool in chemical research, particularly for studying the behavior of organic compounds in different environments. Its unique characteristics can provide insights into molecular interactions, reaction mechanisms, and the development of new chemical methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 6638-91-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6638-91:
(6*6)+(5*6)+(4*3)+(3*8)+(2*9)+(1*1)=121
121 % 10 = 1
So 6638-91-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H19NO/c18-16-14(12-17-10-4-1-5-11-17)9-8-13-6-2-3-7-15(13)16/h2-3,6-9,18H,1,4-5,10-12H2
6638-91-1Relevant articles and documents
An amino-naphthol preparation method of compound
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Paragraph 0055; 0056; 0057; 0058; 0059; 0060, (2017/03/17)
The invention relates to a preparation method for aminonaphthol compound. The method includes the following steps: catalyst, aldehyde compound, secondary amine compound and naphthol are sequentially added into water and react under the temperature condition of 20 DEG C to 80 DEG C, and after reaction is complete, reaction liquid is obtained; the reaction liquid is sequentially extracted, dried, concentrated and separated by column chromatography according to the conventional method, so that product I or product II is obtained, and the structural formula of the product is shown in the figure. The preparation method has the advantages of mild conditions, short reaction time, simple post-processing, high yield and environment-friendliness, can realize mass production and has a good industrial application prospect.
Exploiting tautomerism for switching and signaling
Antonov, Liudmil,Deneva, Vera,Simeonov, Svilen,Kurteva, Vanya,Nedeltcheva, Daniela,Wirz, Jakob
supporting information; experimental part, p. 7875 - 7878 (2010/04/06)
Good form: Attaching a flexible piperidine unit to 4-(phenyldiazenyl) naphthalen-1-ol allows construction of a tautomeric switch, where directed shift of the tautomeric equilibrium can be achieved through protonation and deprotonation (see picture). The developed molecular switch shows acceptable complexation with small alkali- and alkaline-earth-metal ions and forms a promising base for further development of effective molecular sensors.
Intramolecular Interactions I. The Use of Some Mannich Bases of Naphthols as Model Compounds for Intramolecular Hydrogen Bonding
Haslinger, Ernst,Wolschann, Peter
, p. 563 - 574 (2007/10/02)
Some model compounds for intramolecular hydrogen bonding are presented.The nmr, IR, UV and fluorescence spectra are shown to be suited for the study of such hydrogen bonds. - Keywords: Hydrogen bond; Intramolecular proton transfer; Mannich bases
